Evidence map›Paper›PMID 40541045›Full record

ArticleJournal of biomechanics2025

In vivo measurement of vertebral deformation using digital tomosynthesis based digital volume correlation.

Daniel Oravec, Roger Zauel, Michael J Flynn, Sudhaker Rao, Yener N Yeni

Abstract read
In one paragraph

Article in Journal of biomechanics, 2025. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 1 paper.

0numbers the graph read from it
0cells of the map it votes in
1citing papers in PubMed
–field-weighted citation impact
1 · What the graph read from it

What it found

Each row is one number read from the abstract, on the scale the paper reported it, with its interval. Left of the dashed line favours the treatment, right favours the comparator. Under each row is the sentence it came from. New to these charts? A ten-minute tutorial.

The abstract states no effect estimate the extractor could read, or names no intervention and outcome on the map, so this paper lights no cell and moves no belief. It is still indexed, cited and linked below.

2 · The registry

The trial behind it

Trials whose registry record cites this paper, or whose number appears in the abstract. A trial that started after this paper was published is citing it as background, not reporting it.

Neither the registry nor the abstract names a trial number. If this is a trial report, that itself is worth knowing.

3 · Its place in the literature

Who cites it

1 citing paper in PubMed.

  1. Frontiers in bioengineering and biotechnology · 2025
    Article
4 · The record

Corrections and comments

PubMed lists nothing against this paper. Absence here is not a guarantee, only a check that was made.

5 · Who and what money

Authors and funding

5 authors.

Daniel OravecBone and Joint Center, Department of Orthopedic Surgery, Henry Ford Health, Detroit, MI, USA. Electronic address: doravec1@hfhs.org.
Roger ZauelBone and Joint Center, Department of Orthopedic Surgery, Henry Ford Health, Detroit, MI, USA.
Michael J FlynnDepartment of Radiology, Henry Ford Health, Detroit, MI, USA. Electronic address: mikef@rad.hfh.edu.
Sudhaker RaoDivision of Endocrinology, Diabetes and Bone & Mineral Disorders and Bone & Mineral Research Laboratory, Henry Ford Health, Detroit, MI, USA; Henry Ford Health + Michigan State University Health Sciences, Detroit, MI, USA. Electronic address: srao1@hfhs.org.
Yener N YeniBone and Joint Center, Department of Orthopedic Surgery, Henry Ford Health, Detroit, MI, USA; Henry Ford Health + Michigan State University Health Sciences, Detroit, MI, USA. Electronic address: yeni@bjc.hfh.edu.

Funding

A Clinically Viable Noninvasive Method for Direct Measurement of Mechanical Strains in Vertebral BoneR21AR070363 · NIAMS · HENRY FORD HEALTH SYSTEM · PI YENI, YENER N · 2017 to 2018
$363k
NIAMS NIH HHS R21 AR070363
6 · The paper itself

Abstract

Vertebral fractures are the most common type of osteoporotic fracture and associated with significant complications. Timely intervention is important to prevent vertebral fractures, however the current standard for assessing osteoporosis (bone mineral density) is not fully accurate for identifying at-risk individuals. Inspired by a laboratory technique combining microcomputed tomography with mechanical loading for mechanical assessment of extracted bone structures, digital tomosynthesis-based digital volume correlation (DTS-DVC) uses supine and standing DTS images of patients in combination with DVC. The current study evaluated in vivo precision errors, and the utility of DTS-DVC in identifying mechanically compromised vertebrae. Seven patients with vertebral fracture (Fx) and twelve without (NFx) were DTS-imaged, and endplate-to-endplate displacement, stiffness, compliance, and endplate distribution statistics were calculated using supine reference images and images acquired in supine, standing, standing while holding added weight. The in vivo measurement error of DTS-DVC metrics and the extent to which DTS-DVC can measure differences in vertebrae due to loading and presence of vertebral deformity (vertebral fracture) were examined. Total measurement error was low (0.017-0.019 mm), and all measured parameters changed with loading (p < 0.0001 to p < 0.05). Endplate-to-endplate displacement and displacement heterogeneity were significantly higher in fractured vs adjacent intact vertebrae. There were large differences in DVC variables between intact L1 vertebrae of Fx and NFx groups; however, these were not statistically demonstrable. Collectively, results support the in vivo feasibility of DTS-DVC and warrant further investigation. A biomechanics-based assessment of vertebral bone quality is expected to improve our understanding and clinical assessment of vertebral fracture risk.

Indexed as

Lumbar VertebraeSpinal FracturesSpineAgedAged, 80 and overBiomechanical PhenomenaBone DensityFemaleHumansMaleMiddle AgedX-Ray MicrotomographyBone imagingDigital tomosynthesisDigital volume correlationVertebral bone

Identifiers

PMID40541045
PMCPMC12243616

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Registered trials

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Read under generation 80e0d062 · epoch 390. Bibliography from PubMed, PubMed Central and OpenAlex; grants from NIH RePORTER; trial links from ClinicalTrials.gov; estimates, votes and beliefs from the OpenQuestion graph.